Varaico: Literature-Extracted Genetic Variants

Gene:SLC35G5
Variant:p.W103R
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SLC35G5

NM_054028.2:p.W103R

Associated Papers

The clinical and molecular landscape of breast cancer in women of African and South Asian ancestry.

Thorn GJ et al.

Nature Communications, 2025

40394000 (PubMed )
Supplement: 41467_2025_59144_MOESM4_ESM.xlsx › Supplementary_Data_7

Genetic variations and recurrence in stage III Korean colorectal cancer: Insights from tumor-only mutation analysis.

Jeon H et al.

Plos One, 2025

40408428 (PubMed )
Supplement: pone.0323302.s003.xlsx › Sheet1

Comprehensive genetic profiling and molecularly guided treatment for patients with primary CNS tumors.

Kuehn JC et al.

Npj Precision Oncology, 2024

39143272 (PubMed )
Supplement: 41698_2024_674_MOESM2_ESM.xlsx › Supplementary_Data_3

Evolutionary history of adenomas to colorectal cancer in FAP families.

Yang C et al.

Frontiers in Genetics, 2024

39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R10487.xls › SNVIndel

Molecular characterization of sub-frontal recurrent medulloblastomas reveals potential clinical relevance.

Chen Z et al.

Frontiers in Neurology, 2023

37181548 (PubMed )
Supplement: Data_Sheet_2.xlsx › PT1-SNP

NPM1 gene mutations can be confidently identified in blood DNA months before de novo AML onset.

Quiros PM et al.

Blood Advances, 2022

34920452 (PubMed )
Supplement: advancesADV2021005927-suppl1.pdf

Genetic mechanisms of HLA-I loss and immune escape in diffuse large B cell lymphoma.

Fangazio M et al.

Proceedings of the National Academy of Sciences of the United States of America, 2021

34050029 (PubMed )
Supplement: pnas.2104504118.sd06.xlsx › Table_S6

Cutaneous and hepatic vascular lesions due to a recurrent somatic GJA4 mutation reveal a pathway for vascular malformation.

Ugwu N et al.

Hgg Advances, 2021

33912852 (PubMed )
Supplement: mmc2.xlsx › Sheet1

Genomic and Transcriptomic Characterization of Relapsed SCLC Through Rapid Research Autopsy.

Chen HZ et al.

Jto Clinical and Research Reports, 2021

34590014 (PubMed )
Supplement: mmc6.xlsx › Bx

Study of Caspase 8 mutation in oral cancer and adjacent precancer tissues and implication in progression.

Singh R et al.

Plos One, 2020

32492030 (PubMed )
Supplement: pone.0233058.s001.xlsx › RADS17

A glioneuronal tumor with CLIP2-MET fusion.

Chowdhury T et al.

Npj Genomic Medicine, 2020

32550005 (PubMed )
Supplement: 41525_2020_131_MOESM2_ESM.xlsx › Mutation__exonic_splicing_

Comparative sequencing analysis reveals high genomic concordance between matched primary and metastatic colorectal cancer lesions.

Brannon AR et al.

Genome Biology, 2014

25164765 (PubMed )
Supplement: 13059_2014_454_MOESM5_ESM.xlsx › WGS_mutations

Comprehensive genomic analysis of a BRCA2 deficient human pancreatic cancer.

Barber LJ et al.

Plos One, 2011

21750719 (PubMed )
Supplement: pone.0021639.s006.xls › Sheet1
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."